文章基本信息

标题：Cooperative strings and glassy interfaces
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作者：Thomas Salez ; Justin Salez ; Kari Dalnoki-Veress 等
期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2015
卷号：112
期号：27
页码：8227-8231
DOI：10.1073/pnas.1503133112
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：SignificanceAccording to Philip Anderson, the deepest and most interesting unsolved problem in solid-state physics is probably the glass transition. By extension, this includes the highly debated confinement effects in glassy polymer films. The present article introduces a minimal analytical model, which invokes only the ideas of molecular crowding and string-like cooperative rearrangement, before addressing the key effects of interfaces. The validity and simplicity of the approach make it ideal for application to various systems and geometries, and suggest that dynamics in glass-forming materials might be understood from elementary arguments. We introduce a minimal theory of glass formation based on the ideas of molecular crowding and resultant string-like cooperative rearrangement, and address the effects of free interfaces. In the bulk case, we obtain a scaling expression for the number of particles taking part in cooperative strings, and we recover the Adam-Gibbs description of glassy dynamics. Then, by including thermal dilatation, the Vogel-Fulcher-Tammann relation is derived. Moreover, the random and string-like characters of the cooperative rearrangement allow us to predict a temperature-dependent expression for the cooperative length{xi} of bulk relaxation. Finally, we explore the influence of sample boundaries when the system size becomes comparable to{xi} . The theory is in agreement with measurements of the glass-transition temperature of thin polymer films, and allows quantification of the temperature-dependent thickness hm of the interfacial mobile layer.
关键词：glass transition ; cooperative rearrangement ; thin films